Arcinova, A Quotient Sciences Company, is dedicated to providing innovative contract research, development, and manufacturing services. We offer a comprehensive range of integrated specialist services for early stage drug development, underpinned by strong industry knowledge and scientific expertise.
Our mission is to bring science, innovation, and collaboration together to overcome the barriers in drug development. We empower emerging biotechs and large pharma alike to bring life-changing therapies to patients faster, through an efficient, effective approach focused on quality, science, and innovation.
Our vision is to advance progress through science, delivering solutions that make a measurable difference. We look ahead with purpose, driven to shape a smarter, more resilient future for all.
The Role
We are looking for a QA Officer (Operations) for an onsite opportunity in Alnwick.
In this role, you will support and maintain the site’s GxP (GMP, GLP, GCP) Quality Management System.
This is an excellent opportunity for someone with experience in a regulated environment who is looking to further develop their career in Quality Assurance. You will play a vital role in ensuring ongoing compliance with GxP guidelines and regulations, supporting both site operations and audit readiness.
Main Responsibilities
* Support the maintenance of the site’s GxP Quality Management System
* Conduct a programme of internal audits, including:
* Facility audits
* GLP/GCP report and data audits
* Prepare, review, and approve quality documents
* Prepare and review Quality Agreements
* Participate in the Supplier Qualification programme
* Provide support for the eQMS (Veeva)
* Act as QA representative for quality events
* Support customer audits and regulatory inspections, including:
* Coordinating responses
* Tracking corrective actions
* Prepare and deliver GxP training sessions
Skills and Experience Required
* Educated to degree level or equivalent
* Previous experience of working in a GxP environment
* This role will primarily support GCP/ GLPquality assuranceactivities thereforepreviousanalytical/ QC experiencewould behighlyadvantageous
* Good interpersonal and communication skills, both written and oral
* Self‑motivated with the ability to work independently and as part of a team
* Strong attention to detail
* High level of personal integrity and commitment
* Flexible approach to new work challenges and changing priorities
Eligibility to Work in the UK
Please note that this position isnot eligible for sponsorship under the UK points-based immigration system. If you require sponsorship, we will be unable to progress your application or make an offer of employment.
As this is apermanent role, we are also unable to accept applications from candidates on a Graduate Visa.
Application Requirements
When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined.
Our Commitment to Diversity, Equity and Inclusion
Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today.
Specifically we will not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.
This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.
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